Label: HANTAI 8030 CA-D3 GOLD (ostreae concha- calcium 99% tablet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated April 16, 2019

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  • ACTIVE INGREDIENT

    Ostreae Concha (Calcium 99%)

  • INACTIVE INGREDIENT

    Magnesium, Zinc Oxide, Selenium, Germanium, Iron, Potassium, Manganese

  • PURPOSE

    To prevent and cure the osteoporosis, cardiovascular discorders, depression, verve stability, muscle pain, arthritis, menstrual pain, ostalgia and promote growth and healing.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • WARNING

    • Please note it may choke during the intake tablets.
    • Please check product ingredients if you have any allergies before taking.
    • Please be careful during open the product package.
    • Keep product out of direct sunlight, high temperature and humidity.
    • Store in a cool dry place.
    • Keep out of reach of children.
    • Any items past the expiration date or damaged in transit can be exchanged where you originally purchased the item.
  • USES

    Take one tablet every time, two times a day with enough water.

  • INDICATION & USAGE SECTION

    For oral use only

  • PRINCIPAL DISPLAY PANEL

    Hantai 8030 Ca-D3 Gold

  • INGREDIENTS AND APPEARANCE
    HANTAI 8030 CA-D3 GOLD 
    ostreae concha (calcium 99%) tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55259-5001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM (UNII: SY7Q814VUP) (CALCIUM - UNII:SY7Q814VUP) CALCIUM0.99 
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM (UNII: I38ZP9992A)  
    MANGANESE (UNII: 42Z2K6ZL8P)  
    GERMANIUM (UNII: 00072J7XWS)  
    IRON (UNII: E1UOL152H7)  
    POTASSIUM (UNII: RWP5GA015D)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    SELENIUM (UNII: H6241UJ22B)  
    Product Characteristics
    ColorwhiteScorescore with uneven pieces
    ShapeOVALSize12mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55259-5001-11 in 1 PACKAGE04/20/2019
    1120 in 1 BOTTLE; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/18/2015
    Labeler - APEXEL CO., LTD. (687287979)
    Registrant - APEXEL CO., LTD. (687287979)
    Establishment
    NameAddressID/FEIBusiness Operations
    APEXEL CO., LTD.687287979manufacture(55259-5001)
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